載入...
Hyper-IgD syndrome/mevalonate kinase deficiency: what is new?
Mevalonate kinase deficiency or hyper-IgD syndrome is a hereditary autoinflammatory syndrome caused by mutations in the mevalonate kinase gene. In this review, we will discuss new findings in this disorder that have been published in the last 2 years. This includes new insights into pathophysiology,...
Na minha lista:
| 發表在: | Semin Immunopathol |
|---|---|
| Main Authors: | , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Springer Berlin Heidelberg
2015
|
| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4491100/ https://ncbi.nlm.nih.gov/pubmed/25990874 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00281-015-0492-6 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|